Anandamide activates peripheral nociceptors in normal and arthritic rat knee joints

被引:59
作者
Gauldie, SD
McQueen, DS
Pertwee, R
Chessell, IP
机构
[1] Univ Edinburgh, Dept Neurosci, Sensory Pharmacol Unit, Edinburgh EH8 9JZ, Midlothian, Scotland
[2] Univ Aberdeen, Inst Med Sci, Dept Biomed Sci, Aberdeen AD25 2ZD, Scotland
[3] Univ Cambridge, Glaxo Inst Appl Pharmacol, Dept Pharmacol, Cambridge CB2 1QJ, England
关键词
sensory nerves; anandamide; adjuvant arthritis; knee joint; afferent nociceptors; vanilloid receptor;
D O I
10.1038/sj.bjp.0703890
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
The effects of the endogenous cannabinoid anandamide were studied on peripheral, polymodal nociceptors recorded from normal and chronically inflamed (Freund's adjuvant) knee joint afferents in rats anaesthetized with pentobarbitone. Anandamide (560 nmol) caused a rapid, short lasting excitation of a sub-population of capsaicin-sensitive nociceptive afferents in normal knee joints (7.2+/-2.3 impulses s(-1); n = 15 units from five animals). In arthritic joints there were 9.7+/-3.0 impulses s(-1) (n=11 from six animals), which was not significantly different from normal joints. The excitation was dose dependent (8.6 - 2900 nmol) and mediated by activation of the vanilloid receptor (VR1) as it was abolished by the VR1 antagonist capsazepine (1 mg kg(-1)). Our results show that anandamide, at high doses, can activate nociceptive afferents innervating the rat knee joints, in contrast with its widely described analgesic actions.
引用
收藏
页码:617 / 621
页数:5
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